WO2000031783A1 - Fabrication de couches de nitrure de gallium sur du silicium - Google Patents
Fabrication de couches de nitrure de gallium sur du silicium Download PDFInfo
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- WO2000031783A1 WO2000031783A1 PCT/US1999/027358 US9927358W WO0031783A1 WO 2000031783 A1 WO2000031783 A1 WO 2000031783A1 US 9927358 W US9927358 W US 9927358W WO 0031783 A1 WO0031783 A1 WO 0031783A1
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- Prior art keywords
- layer
- gallium nitride
- silicon
- silicon carbide
- growing
- Prior art date
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- 229910002601 GaN Inorganic materials 0.000 title claims abstract description 412
- JMASRVWKEDWRBT-UHFFFAOYSA-N Gallium nitride Chemical compound [Ga]#N JMASRVWKEDWRBT-UHFFFAOYSA-N 0.000 title claims abstract description 254
- 229910052710 silicon Inorganic materials 0.000 title claims abstract description 192
- 239000010703 silicon Substances 0.000 title claims abstract description 192
- 238000004519 manufacturing process Methods 0.000 title claims description 22
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims abstract description 195
- 239000000758 substrate Substances 0.000 claims abstract description 143
- 229910010271 silicon carbide Inorganic materials 0.000 claims abstract description 142
- 238000004377 microelectronic Methods 0.000 claims abstract description 113
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 10
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 10
- 239000001301 oxygen Substances 0.000 claims abstract description 10
- 239000012212 insulator Substances 0.000 claims abstract description 6
- 239000010410 layer Substances 0.000 claims description 539
- 238000000034 method Methods 0.000 claims description 62
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 26
- PMHQVHHXPFUNSP-UHFFFAOYSA-M copper(1+);methylsulfanylmethane;bromide Chemical compound Br[Cu].CSC PMHQVHHXPFUNSP-UHFFFAOYSA-M 0.000 claims description 23
- 239000002344 surface layer Substances 0.000 claims description 16
- 239000000377 silicon dioxide Substances 0.000 claims description 13
- 235000012239 silicon dioxide Nutrition 0.000 claims description 12
- NJPPVKZQTLUDBO-UHFFFAOYSA-N novaluron Chemical compound C1=C(Cl)C(OC(F)(F)C(OC(F)(F)F)F)=CC=C1NC(=O)NC(=O)C1=C(F)C=CC=C1F NJPPVKZQTLUDBO-UHFFFAOYSA-N 0.000 claims description 11
- 239000002243 precursor Substances 0.000 claims description 11
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 6
- 229910052799 carbon Inorganic materials 0.000 claims description 6
- 150000004767 nitrides Chemical class 0.000 claims 1
- 230000012010 growth Effects 0.000 abstract description 109
- 208000012868 Overgrowth Diseases 0.000 abstract description 18
- 238000000926 separation method Methods 0.000 abstract description 2
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 35
- 230000007547 defect Effects 0.000 description 18
- 239000004065 semiconductor Substances 0.000 description 17
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 description 11
- 229910052733 gallium Inorganic materials 0.000 description 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
- 238000009792 diffusion process Methods 0.000 description 9
- 230000015572 biosynthetic process Effects 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- 235000012431 wafers Nutrition 0.000 description 7
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 5
- 230000004888 barrier function Effects 0.000 description 5
- 238000001816 cooling Methods 0.000 description 5
- 239000001257 hydrogen Substances 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- 230000005693 optoelectronics Effects 0.000 description 5
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 4
- 238000007796 conventional method Methods 0.000 description 4
- 239000003085 diluting agent Substances 0.000 description 4
- 238000000407 epitaxy Methods 0.000 description 4
- 229910052738 indium Inorganic materials 0.000 description 4
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 4
- 230000007246 mechanism Effects 0.000 description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 description 4
- 230000006911 nucleation Effects 0.000 description 4
- 238000010899 nucleation Methods 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- 238000000927 vapour-phase epitaxy Methods 0.000 description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
- 239000005977 Ethylene Substances 0.000 description 3
- 229910052581 Si3N4 Inorganic materials 0.000 description 3
- 229910045601 alloy Inorganic materials 0.000 description 3
- 239000000956 alloy Substances 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000005530 etching Methods 0.000 description 3
- 230000003993 interaction Effects 0.000 description 3
- 238000004518 low pressure chemical vapour deposition Methods 0.000 description 3
- 238000001465 metallisation Methods 0.000 description 3
- 229910000069 nitrogen hydride Inorganic materials 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 3
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000010408 film Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 230000010354 integration Effects 0.000 description 2
- 238000002488 metal-organic chemical vapour deposition Methods 0.000 description 2
- 230000000877 morphologic effect Effects 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 125000002524 organometallic group Chemical group 0.000 description 2
- 239000001294 propane Substances 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 229910000077 silane Inorganic materials 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000010409 thin film Substances 0.000 description 2
- 239000012808 vapor phase Substances 0.000 description 2
- JBRZTFJDHDCESZ-UHFFFAOYSA-N AsGa Chemical compound [As]#[Ga] JBRZTFJDHDCESZ-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 229910000807 Ga alloy Inorganic materials 0.000 description 1
- 229910001218 Gallium arsenide Inorganic materials 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- RNQKDQAVIXDKAG-UHFFFAOYSA-N aluminum gallium Chemical compound [Al].[Ga] RNQKDQAVIXDKAG-UHFFFAOYSA-N 0.000 description 1
- AJGDITRVXRPLBY-UHFFFAOYSA-N aluminum indium Chemical compound [Al].[In] AJGDITRVXRPLBY-UHFFFAOYSA-N 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 238000005229 chemical vapour deposition Methods 0.000 description 1
- 238000004581 coalescence Methods 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 230000002860 competitive effect Effects 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 239000012776 electronic material Substances 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hcl hcl Chemical compound Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 230000000873 masking effect Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000000059 patterning Methods 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 238000000206 photolithography Methods 0.000 description 1
- 231100000572 poisoning Toxicity 0.000 description 1
- 230000000607 poisoning effect Effects 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 230000001902 propagating effect Effects 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 229910052594 sapphire Inorganic materials 0.000 description 1
- 239000010980 sapphire Substances 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 238000005476 soldering Methods 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- 230000008646 thermal stress Effects 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
- RGGPNXQUMRMPRA-UHFFFAOYSA-N triethylgallium Chemical compound CC[Ga](CC)CC RGGPNXQUMRMPRA-UHFFFAOYSA-N 0.000 description 1
- 229910052984 zinc sulfide Inorganic materials 0.000 description 1
Classifications
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- H01L29/00—Semiconductor devices adapted for rectifying, amplifying, oscillating or switching, or capacitors or resistors with at least one potential-jump barrier or surface barrier, e.g. PN junction depletion layer or carrier concentration layer; Details of semiconductor bodies or of electrodes thereof ; Multistep manufacturing processes therefor
- H01L29/02—Semiconductor bodies ; Multistep manufacturing processes therefor
- H01L29/12—Semiconductor bodies ; Multistep manufacturing processes therefor characterised by the materials of which they are formed
- H01L29/20—Semiconductor bodies ; Multistep manufacturing processes therefor characterised by the materials of which they are formed including, apart from doping materials or other impurities, only AIIIBV compounds
- H01L29/2003—Nitride compounds
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- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
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- H01L21/02367—Substrates
- H01L21/0237—Materials
- H01L21/02373—Group 14 semiconducting materials
- H01L21/02381—Silicon, silicon germanium, germanium
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- H01L21/02439—Materials
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- H01L21/02447—Silicon carbide
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- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
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- H01L21/02494—Structure
- H01L21/02496—Layer structure
- H01L21/02502—Layer structure consisting of two layers
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- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
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- H01L29/267—Semiconductor bodies ; Multistep manufacturing processes therefor characterised by the materials of which they are formed including, apart from doping materials or other impurities, elements provided for in two or more of the groups H01L29/16, H01L29/18, H01L29/20, H01L29/22, H01L29/24, e.g. alloys in different semiconductor regions, e.g. heterojunctions
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Definitions
- This invention relates to microelectronic devices and fabrication methods, and more particularly to gallium nitride semiconductor devices and fabrication methods therefor.
- gallium nitride is being widely investigated for microelectronic devices including but not limited to transistors, field emitters and optoelectronic devices. It will be understood that, as used herein, gallium nitride also includes alloys of gallium nitride such as aluminum gallium nitride, indium gallium nitride and aluminum indium gallium nitride.
- a major problem in fabricating gallium nitride-based microelectronic devices is the fabrication of gallium nitride semiconductor layers having low defect densities. It is known that one contributor to defect density is the substrate on which the gallium nitride layer is grown. Accordingly, although gallium nitride layers have been grown on sapphire substrates, it is known to reduce defect density by growing gallium nitride layers on aluminum nitride buffer layers which are themselves formed on silicon carbide substrates. Notwithstanding these advances, continued reduction in defect density is desirable.
- This technique often is referred to as "Epitaxial Lateral Overgrowth" (ELO).
- ELO Epiaxial Lateral Overgrowth
- the layer of gallium nitride may be laterally grown until the gallium nitride coalesces on the mask to form a single layer on the mask.
- a second mask may be formed on the laterally overgrown gallium nitride layer, that includes at least one opening that is offset from the underlying mask. ELO then again is performed through the openings in the second mask to thereby overgrow a second low defect density continuous gallium nitride layer. Microelectronic devices then may be formed in this second overgrown layer.
- ELO of gallium nitride is described, for example, in the publications entitled Lateral Epitaxy of Low Defect Density GaN Layers Via Organometallic Vapor Phase Epitaxy to Nam et al., Appl. Phys. Lett. Vol. 71, No.
- ELO and pendeoepitaxy can provide relatively large, low defect gallium nitride layers for microelectronic applications.
- a major concern that may limit the mass production of gallium nitride devices is the growth of the gallium nitride layers on a silicon carbide substrate.
- silicon carbide substrates still may be relatively expensive compared to conventional silicon substrates.
- silicon carbide substrates generally are smaller than silicon substrates, which can reduce the number of devices that can be formed on a wafer.
- large investments are being made in silicon carbide processing equipment, even larger investments already have been made in conventional silicon substrate processing equipment. Accordingly, the use of an underlying silicon carbide substrate for fabricating gallium nitride microelectronic structures may adversely impact the cost and/or availability of gallium nitride devices.
- the present invention provides methods of fabricating a gallium nitride microelectronic layer by converting a surface of a (111) silicon layer to 3C-silicon carbide. A layer of 3C-silicon carbide is then epitaxially grown on the converted surface of the (111) silicon layer. A layer of 2H-gallium nitride then is grown on the epitaxially grown layer of 3C-silicon carbide. The layer of 2H-gallium nitride then is laterally grown to produce the gallium nitride microelectronic layer.
- the silicon layer is a (111) silicon substrate, the surface of which is converted to 3C-silicon carbide.
- the (111) silicon layer is part of a Separation by IMplanted OXygen (SIMOX) silicon substrate which includes a layer of implanted oxygen that defines the (111) layer on the (111) silicon substrate.
- the (111) silicon layer is a portion of a Silicon- On-Insulator (SOI) substrate in which a (111) silicon layer is bonded to a substrate.
- SOI Silicon- On-Insulator
- the present invention can use conventional bulk silicon, SIMOX and SOI substrates as a base or platform for fabricating a gallium nitride microelectronic layer.
- conventional silicon technology low cost and/or large area silicon substrates may be used and conventional silicon wafer processing systems also may be used. Accordingly, low cost and/or high volume production of gallium nitride microelectronic layers may be provided.
- the surface of the (111) silicon layer preferably is converted to 3C-silicon carbide by chemically reacting the surface of the (111) silicon layer with a carbon containing precursor such as ethylene, to convert the surface of the (111) silicon layer to 3C-silicon carbide.
- the layer of 3C-silicon carbide then may be epitaxially grown on the converted surface using standard vapor phase epitaxial techniques for silicon carbide. Alternatively, the layer of 3C-silicon carbide may be grown directly on the (111) silicon layer, without the need for conversion.
- the epitaxially grown layer of 3C-silicon carbide may be thinned.
- an aluminum nitride and/or gallium nitride buffer layer preferably is grown on the epitaxially grown layer of 3C-silicon carbide.
- the gallium nitride then is grown on the buffer layer, opposite the epitaxially grown layer of 3C-silicon carbide.
- Lateral growth of the layer of 2H-gallium nitride may be performed by ELO wherein a mask is formed on the layer of 2H-gallium nitride, the mask including at least one opening that exposes the layer of 2H-gallium nitride.
- the layer of 2H- gallium nitride then is laterally grown through the at least one opening and onto the mask.
- a second, offset mask also may be formed on the laterally grown layer of 2H- gallium nitride and a second laterally grown layer of 2H-gallium nitride may be overgrown onto the offset mask.
- Lateral growth of the layer of 2H-gallium nitride also may be performed using pendeoepitaxial techniques wherein at least one trench and/or post is formed in a layer of 2H-gallium nitride to define at least one sidewall therein.
- the layer of 2H-gallium nitride then is laterally grown from the at least one sidewall.
- Pendeoepitaxial lateral growth preferably continues until the laterally grown sidewalls coalesce on the top of the posts or trenches.
- the top of the posts and/or the trench floors may be masked to promote lateral growth and reduce nucleation and vertical growth.
- the trenches preferably extend into the silicon carbide layer to also reduce nucleation and vertical growth.
- the present invention can use bulk silicon substrates, SIMOX substrates or SOI substrates as a platform for gallium nitride fabrication. Preferred methods using each of these substrates now will be described.
- the surface of the (1 11) silicon substrate preferably is converted to 3C-silicon carbide and a layer of 3C-silicon carbide then is epitaxially grown on the converted surface of the (111) silicon substrate.
- the epitaxially grown layer of 3C-silicon carbide may be thinned.
- An aluminum nitride and/or gallium nitride buffer layer is grown on the epitaxially grown layer of 3C- silicon carbide.
- a layer of 2H-gallium nitride is grown on the buffer layer.
- the layer of 2H-gallium nitride then is laterally grown to produce the gallium nitride microelectronic layer.
- the lateral growth may proceed using ELO, pendeoepitaxy and/or other techniques.
- oxygen is implanted into a (111) silicon substrate to form a buried silicon dioxide layer that defines a (1 1 1) silicon surface layer on the (111) silicon substrate. At least a portion of the (111) silicon surface layer, and preferably all of the (111) silicon surface layer, is converted to 3C-silicon carbide. A layer of 3C-silicon carbide then is epitaxially grown on the converted (1 1 1) silicon surface layer. The epitaxially grown layer of 3C-silicon carbide then may be thinned and an aluminum nitride and/or gallium nitride buffer layer is grown on the epitaxially grown layer of 3C-silicon carbide.
- a layer of 2H-gallium nitride then is grown on the buffer layer.
- the layer of 2H-gallium nitride then is laterally grown, using ELO, pendeoepitaxy and/or other techniques to produce the gallium nitride microelectronic layer.
- a (111) silicon substrate is bonded to another substrate, preferably a (100) silicon substrate.
- the (111) silicon substrate is thinned to define a (111) silicon layer on the (100) silicon substrate. At least a portion, and preferably all, of the (111) silicon layer is converted to 3C-silicon carbide.
- a layer of 3C-silicon carbide is epitaxially grown on the converted (111) silicon layer.
- the epitaxially grown layer of 3C-silicon carbide may be thinned and an aluminum nitride and/or gallium nitride buffer layer is grown on the epitaxially grown layer of 3C-silicon carbide.
- a layer of 2H-gallium nitride then is grown on the buffer layer and the layer of 2H-gallium nitride is laterally grown, using ELO, pendeoepitaxy and/or other techniques to produce the gallium nitride microelectronic layer.
- microelectronic devices also may be formed in the (100) silicon substrate, prior to or after forming the gallium nitride microelectronic layer.
- a portion of the (11 1) silicon layer, the 3C-silicon carbide layer, the gallium nitride layer and the gallium nitride microelectronic layer may be removed to expose the microelectronic devices in the (100) silicon substrate.
- an epitaxial silicon layer may be grown from the exposed portion of the (100) silicon substrate, and microelectronic devices may be formed in the epitaxial silicon layer.
- the gallium nitride structures may be capped prior to forming the epitaxial silicon layer.
- optoelectronic devices may be formed in the gallium nitride layer whereas conventional CMOS or other microelectronic devices may be formed in the (100) silicon substrate. Integrated optoelectronic substrates thereby may be formed.
- gallium nitride microelectronic structures preferably comprise a (111) silicon layer, a 3C-silicon carbide layer on the (11 1) silicon layer, an underlying layer of 2H-gallium nitride on the 3C-silicon carbide layer and a lateral layer of 2H-gallium nitride on the underlying layer of 2H- gallium nitride.
- the (111) silicon layer may comprise a surface of a (11 1) bulk silicon substrate, a surface of a (111) SIMOX substrate or a surface of a (111) SOI substrate.
- a buffer layer of aluminum nitride and/or gallium nitride may be provided between the 3C-silicon carbide layer and the underlying layer of 2H-gallium nitride.
- a mask may be provided on the underlying layer of 2H-gallium nitride, the mask including at least one opening that exposes the underlying layer of 2H-gallium nitride, and the lateral layer of 2H-gallium nitride extending through the at least one opening and onto the mask.
- a second laterally offset mask and a second lateral layer of 2H-gallium nitride also may be provided.
- At least one trench and/or post may be provided in the underlying layer of 2H-gallium nitride that defines at least one sidewall in the underlying layer of 2H-gallium nitride, and the lateral layer of 2H-gallium nitride may extend from the at least one sidewall.
- the lateral layer of 2H-gallium nitride may extend onto the post tops, which may be masked or unmasked.
- the trench bottoms also may be masked or the trench may extend through the aluminum nitride layer into the silicon carbide layer.
- a preferred embodiment using a (111) bulk silicon substrate includes a 3C- silicon carbide layer on the (1 11) silicon substrate, a buffer layer of aluminum nitride and/or gallium nitride on the 3C-silicon carbide layer, an underlying layer of 2H- gallium nitride on the buffer layer and a lateral layer of 2H-gallium nitride on the underlying layer of 2H-gallium nitride.
- a preferred embodiment using a SIMOX substrate includes a (111) silicon substrate, a silicon dioxide layer on the (11 1) silicon substrate, a 3C-silicon carbide layer on the silicon dioxide layer, a buffer layer of aluminum nitride and/or gallium nitride on the 3C-silicon carbide layer, an underlying layer of 2H-gallium nitride on the buffer layer and a lateral layer of 2H-gallium nitride on the underlying layer of 2H-gallium nitride.
- a preferred embodiment using an SOI substrate includes a (100) silicon substrate, an insulating layer on the (100) silicon substrate, a 3C-silicon carbide layer on the insulating layer, a buffer layer of aluminum nitride and/or gallium nitride on the 3C-silicon carbide layer, an underlying layer of 2H-gallium nitride on the buffer layer and a lateral layer of 2H-gallium nitride on the underlying layer of 2H-gallium nitride.
- a plurality of microelectronic devices preferably are formed in the (100) silicon substrate.
- the 3C- silicon carbide layer, the layer of aluminum nitride, the underlying layer of 2H- gallium nitride and the lateral layer of 2H-gallium nitride preferably define a pedestal that exposes the plurality of microelectronic devices in the (100) silicon substrate.
- the pedestal may expose the (100) silicon substrate, substrate, a (100) silicon layer may be included on the exposed portion of the (100) silicon substrate, and the microelectronic devices may be formed in the (100) silicon layer.
- a layer of (1 11) silicon may be present between the insulating layer and the 3C-silicon carbide layer.
- gallium nitride microelectronic structures may be formed on commonly used bulk silicon, SIMOX and SOI substrates. Low cost and/or high availability gallium nitride devices thereby may be provided. Integration with conventional CMOS or other silicon technologies also may be facilitated.
- Figures 1-14 are cross-sectional views of first gallium nitride microelectronic structures during intermediate fabrication steps, according to the present invention.
- Figures 16-26 are cross-sectional views of second gallium nitride microelectronic structures during intermediate fabrication steps, according to the present invention.
- Figures 27-41 are cross-sectional views of third gallium nitride microelectronic structures during intermediate fabrication steps, according to the present invention.
- Figures 42-43 are cross-sectional views of fourth gallium nitride microelectronic structures during intermediate fabrication steps, according to the present invention.
- Figures 44-45 are cross-sectional views of fifth gallium nitride microelectronic structures during intermediate fabrication steps, according to the present invention.
- Figure 46 is a cross-sectional view of sixth gallium nitride microelectronic structures according to the present invention.
- Figures 47-49 are cross-sectional views of seventh gallium nitride microelectronic structures during intermediate fabrication steps, according to the present invention.
- FIG. 1 first embodiments of methods of fabricating gallium nitride microelectronic layers and microelectronic structures formed thereby are illustrated.
- a bulk silicon (1 11) substrate 102a is provided.
- the crystallographic designation conventions used herein are well known to those having skill in the art, and need not be described further.
- the surface of the (111) silicon substrate 102a preferably is converted to 3C-silicon carbide 102b.
- the surface of the silicon substrate 102a may be converted to 3C-silicon carbide by exposure to one or more carbon-containing sources.
- a converted layer of 3C-SiC may be formed by heating the bulk silicon substrate 102a using ethylene at about 925°C for about fifteen minutes at a pressure of about 5E-5 Torr. More preferably, an ethylene flow rate of about 0.5sccm is used while heating the substrate from room temperature to about 925°C at a ramp up rate of about 30°C per minute and holding at about 925°C for about fifteen minutes and at about 5E-5 Torr, resulting in a thin, 50 Angstrom, 3C-silicon carbide layer 102b.
- a layer of 3C-silicon carbide 102c may be formed on the converted 3C-silicon carbide layer 102b using conventional vapor phase epitaxial techniques.
- the silicon carbide layer may be grown using propane (about 15% in hydrogen) and silane (about 5% in hydrogen) at about 1360°C and about 760 Torr. More preferably, propane (about 15% in hydrogen) at about 25 seem, silane (about 5% in hydrogen) at about 100 seem and hydrogen gas at about 2500 seem at a temperature of about 1360°C and pressure of about 760 Torr may be used.
- propane about 15% in hydrogen
- silane about 5% in hydrogen
- the surface of the silicon substrate need not be converted to 3C-silicon carbide prior to forming silicon carbide layer 102c. Rather, layer 102c may be formed directly on the silicon substrate 102a.
- the epitaxially grown layer of 3C-silicon carbide 102c may be thinned, for example, to a thickness of about 0.5 ⁇ m, to form a thin layer 102c' of 3C-silicon carbide. Thinning may take place using chemical mechanical polishing. The thinning may promote the formation of a smooth, defect free nucleation surface for 2H-aluminum nitride as will be described below. However, it will be understood that the 3C-silicon carbide layer 102c need not be thinned.
- a buffer layer of 2H-aluminum nitride and/or gallium nitride 102d then is grown on the epitaxially grown layer of 3C-silicon carbide 102c or 102c'.
- the aluminum nitride layer 102d may be about 0.01 ⁇ m thick and may be formed using conventional techniques such as metalorganic vapor phase epitaxy. It also will be understood that the buffer layer of aluminum nitride and/or gallium nitride 102d need not be included, and gallium nitride may be formed directly on the epitaxially grown layer 102c/102c' of 3C-silicon carbide.
- the combination of the (111) silicon substrate 102a, the silicon carbide layers 102b and 102c' and the buffer layer 102d forms a platform 102 upon which a gallium nitride microelectronic layer may be fabricated.
- a gallium nitride microelectronic layer may be fabricated.
- an underlying 2H-gallium nitride layer 104 is grown on the 2H-aluminum nitride layer 102d.
- the gallium nitride layer 104 may be between about 0.5 and about 2.0 ⁇ m thick and may be grown at about 1000°C in a cold wall vertical and inductively heated metal organic vapor phase epitaxy system using triethyl gallium at about 26 m ⁇ mol/min, ammonia at about 1500 seem and about 3000 seem hydrogen diluent. Additional details of the growth technique for the aluminum nitride layer 102d and the gallium nitride layer 104 may be found in a publication by T. W. Weeks et al.
- gallium nitride microelectronic layers may be fabricated on the underlying gallium nitride layer 104 using ELO. It also will be understood, however, that gallium nitride microelectronic layers may be fabricated using pendeoepitaxy as will be described in connection with other embodiments of the invention and/or using other techniques for fabricating gallium nitride microelectronic layers.
- the underlying gallium nitride layer 104 is masked with a first mask 106 that includes a first array of openings 107 therein.
- the first mask may comprise silicon dioxide at a thickness of 1000A and may be deposited using Low Pressure Chemical Vapor Deposition (LPCVD) at 410°C. Other masking materials may be used.
- the first mask may be patterned using standard photolithography techniques and etching in a buffered HF solution.
- the first openings 107 are 3 ⁇ m-wide openings that extend in parallel at distances of between 3 and 40 ⁇ m and that are oriented along the ⁇ 1 1 00 > direction on the underlying gallium nitride layer 104.
- the structure Prior to further processing, the structure may be dipped in a 50% buffered hydrochloric acid (HCl) solution to remove surface oxides from the underlying gallium nitride layer 104.
- HCl 50% buffered hydrochloric acid
- the underlying gallium nitride layer 104 is grown through the first array of openings 107 to form first vertical gallium nitride layer 108a in the first openings.
- Growth of gallium nitride may be obtained at 1000-1100°C and 45 Torr.
- the precursors TEG at 13-39 ⁇ mol/min and NH 3 at 1500 seem may be used in combination with a 3000 seem H diluent. If gallium nitride alloys are formed, additional conventional precursors of aluminum or indium, for example, may also be used.
- the first gallium nitride layer 108a grows vertically to the top of the first mask 106.
- underlying gallium nitride layer 104 also may be grown laterally without using a mask 106, by appropriately controlling growth parameters and/or by appropriately patterning the underlying gallium nitride layer 104.
- a patterned layer may be formed on the underlying gallium nitride layer after vertical growth or lateral growth, and need not function as a mask.
- lateral growth in two dimensions may be used to form an overgrown gallium nitride semiconductor layer.
- mask 106 may be patterned to include an array of openings 107 that extend along two orthogonal directions such as ⁇ 1100 > and ⁇ 1120 > .
- the openings can form a rectangle of orthogonal striped patterns.
- the ratio of the edges of the rectangle is preferably proportional to the ratio of the growth rates of the ⁇ 1120 ⁇ and
- ⁇ 1101 ⁇ facets for example, in a ratio of 1.4: 1.
- first gallium nitride layer 108a causes lateral overgrowth onto the first mask 106, to form first lateral gallium nitride layer 108b. Growth conditions for overgrowth may be maintained as was described in connection with Figure 8.
- lateral overgrowth is optionally allowed to continue until the lateral growth fronts coalesce at first interfaces 108c, to form a first continuous gallium nitride layer 108.
- the total growth time may be approximately 60 minutes.
- Microelectronic devices may be formed in the first continuous gallium nitride layer 108.
- the first vertical gallium nitride layer 108a is masked with a second mask 206 that includes a second array of openings 207 therein.
- the second mask may be fabricated as was described in connection with the first mask.
- the second mask may also be eliminated, as was described in connection with the first mask of Figure 8.
- the second mask 206 preferably covers the entire first vertical gallium nitride layer 108a, so as to prevent defects therein from propagating vertically or laterally.
- mask 206 may extend onto first lateral gallium nitride layer 108b as well.
- the first lateral gallium nitride layer 108c is grown vertically through the second array of openings 207, to form second vertical gallium nitride layer 208a in the second openings. Growth may be obtained as was described in connection with Figure 8.
- second gallium nitride layer 208a causes lateral overgrowth onto the second mask 206, to form second lateral gallium nitride layer 208b.
- Lateral growth may be obtained as was described in connection with Figure 8.
- lateral overgrowth preferably continues until the lateral growth fronts coalesce at second interfaces 208c to form a second continuous gallium nitride layer 208.
- Total growth time may be approximately 60 minutes.
- Microelectronic devices may then be formed in regions 208a and in regions 208b as shown in Figure 15, because both of these regions are of relatively low defect density. Devices may bridge these regions as well, as shown. Accordingly, a continuous device quality gallium nitride layer 208 may be formed.
- the openings 107 and 207 in the masks are preferably rectangular stripes that preferably extend along the ⁇ 1120 > and/or ⁇ 1 1 00 > directions relative to the underlying gallium nitride layer 104.
- Truncated triangular stripes having (1 1 01) slant facets and a narrow (0001) top facet may be obtained for mask openings 107 and 207 along the ⁇ 1120 > direction.
- Rectangular stripes having a (0001) top facet, (1120) vertical side faces and (1 1 01) slant facets may be grown along the ⁇ 1 1 00 > direction. For growth times up to 3 minutes, similar morphologies may be obtained regardless of orientation. The stripes develop, into different shapes if the growth is continued.
- the amount of lateral growth generally exhibits a strong dependence on stripe orientation.
- the lateral growth rate of the ⁇ 1 1 00 > oriented stripes is generally much faster than those along ⁇ 1120 > . Accordingly, it is most preferred to orient the openings 107 and 207 so that they extend along the ⁇ 1 1 00 > direction of the underlying gallium nitride layer 104.
- Stripes oriented along ⁇ 1 120 > may have wide (1 1 00) slant facets and either a very narrow or no (0001) top facet depending on the growth conditions.
- (1 1 01) is the most stable plane in the gallium nitride wurtzite crystal structure, and the growth rate of this plane is lower than that of others.
- the ⁇ 1 1 01 ⁇ planes of the ⁇ 1 1 00 > oriented stripes may be wavy, which implies the existence of more than one Miller index. It appears that competitive growth of selected ⁇ 1 1 01 ⁇ planes occurs during the deposition which causes these planes to become unstable and which causes their growth rate to increase relative to that of the (1 1 01) of stripes oriented along ⁇ 1120 >.
- the morphologies of the gallium nitride layers selectively grown on openings oriented along ⁇ 1 1 00 > are also generally a strong function of the growth temperatures.
- Layers grown at 1000°C may possess a truncated triangular shape. This morphology may gradually change to a rectangular cross-section as the growth temperature is increased. This shape change may occur as a result of the increase in the diffusion coefficient and therefore the flux of the gallium species along the (0001) top plane onto the ⁇ 1 1 01 ⁇ planes with an increase in growth temperature. This may result in a decrease in the growth rate of the (0001) plane and an increase in that of the ⁇ 1 1 01 ⁇ . This phenomenon has also been observed in the selective growth of gallium arsenide on silicon dioxide. Accordingly, temperatures of 1100°C appear to be most preferred.
- the morphological development of the gallium nitride regions also appears to depend on the flow rate of the TEG.
- An increase in the supply of TEG generally increases the growth rate of the stripes in both the lateral and the vertical directions.
- the lateral/vertical growth rate ratio decrease from 1.7 at the TEG flow rate of 13 ⁇ mol/min to 0.86 at 39 ⁇ mol.min.
- This increased influence on growth rate along ⁇ 0001> relative to that of ⁇ 1120 > with TEG flow rate may be related to the type of reactor employed, wherein the reactant gases flow vertically and pe ⁇ endicular to the substrate.
- gallium nitride layers 108 and 208 may be obtained using 3 ⁇ m wide stripe openings 107 and 207 spaced 7 ⁇ m apart and oriented along ⁇ 1 1 00 > , at 1 100°C and a TEG flow rate of 26 ⁇ mol/min.
- the overgrown gallium nitride layers 108b and 208b may include subsurface voids that form when two growth fronts coalesce.
- the coalesced gallium nitride layers 108 and 208 may have a microscopically flat and pit-free surface.
- the surfaces of the laterally grown gallium nitride layers may include a terrace structure having an average step height of 0.32nm. This terrace structure may be related to the laterally grown gallium nitride, because it is generally not included in much larger area films grown only on aluminum nitride buffer layers.
- the average RMS roughness values may be similar to the values obtained for the underlying gallium nitride layers 104.
- Threading dislocations originating from the interface between the gallium nitride underlayer 104 and the buffer layer 102b, appear to propagate to the top surface of the first vertical gallium nitride layer 108a within the first openings 107 of the first mask 106.
- the dislocation density within these regions is approximately 10 cm " .
- threading dislocations do not appear to readily propagate into the first overgrown regions 108b. Rather, the first overgrown gallium nitride regions 108b contain only a few dislocations. These few dislocations may be formed parallel to the (0001) plane via the extension of the vertical threading dislocations after a 90° bend in the regrown region.
- both the second vertical gallium nitride layer 208a and the second lateral gallium nitride layer 208b propagate from the low defect first overgrown gallium nitride layer 108b, the entire layer 208 can have low defect density.
- the formation mechanism of the selectively grown gallium nitride layer is lateral epitaxy.
- the two main stages of this mechanism are vertical growth and lateral growth.
- Ga or N atoms should not readily bond to the mask surface in numbers and for a time sufficient to cause gallium nitride nuclei to form. They would either evaporate or diffuse along the mask surface to the openings 107 or 207 in the masks or to the vertical gallium nitride surfaces 108a or 208a which have emerged. During lateral growth, the gallium nitride grows simultaneously both vertically and laterally over the mask from the material which emerges over the openings.
- lateral cracking within the SiO may take place due to thermal stresses generated on cooling.
- the viscosity (p) of the SiO at 1050°C is about 10 ' poise which is one order of magnitude greater than the strain point (about 10 1 ' poise) where stress relief in a bulk amo ⁇ hous material occurs within approximately six hours.
- the SiO 2 mask may provide limited compliance on cooling.
- chemical bonding may occur only when appropriate pairs of atoms are in close proximity. Extremely small relaxations of the silicon and oxygen and gallium and nitrogen atoms on the respective surfaces and/or within the bulk of the SiO may accommodate the gallium nitride and cause it to bond to the oxide.
- regions of lateral epitaxial overgrowth through mask openings from an underlying gallium nitride layer may be achieved via MOVPE.
- the growth may depend strongly on the opening orientation, growth temperature and TEG flow rate.
- Coalescence of overgrown gallium nitride regions to form regions with both extremely low densities of dislocations and smooth and pit-free surfaces may be achieved through 3 ⁇ m wide mask openings spaced 7 ⁇ m apart and extending along the ⁇ 1 1 00 > direction, at 1100°C and a TEG flow rate of 26 ⁇ mol/min.
- the lateral overgrowth of gallium nitride via MOVPE may be used to obtain low defect density continuous gallium nitride layers for microelectronic devices.
- the embodiments of Figures 1-15 can use bulk (111) silicon substrate 102a, a 3C-silicon carbide layer 102b/102c' and a buffer layer 102d as a platform 102 on which to grow high quality gallium nitride microelectronic layers.
- the silicon carbide layer 102b/102c' may be critical to the success of forming gallium nitride structures according to the present invention.
- silicon carbide is a preferred material template on which to grow the buffer layer 102d and the gallium nitride semiconductor layer 104.
- the silicon carbide layer may provide a diffusion barrier to prevent the interaction of silicon atoms with gallium and nitrogen species found in the growth environment.
- the silicon atoms from the silicon substrate may have sufficient energy and mobility to diffuse to the surface of the aluminum nitride buffer layer and to react with the gallium and nitrogen species in the growth environment. This may result in the formation of large voids in the underlying silicon substrate and in the "poisoning" of the gallium nitride growth, which may result in the undesirable formation of poly crystalline gallium nitride-containing structures.
- Figures 16-26 second embodiments of fabricating gallium nitride microelectronic layers according to the present invention will be described.
- the embodiments of Figures 16-26 begin with a (111) silicon SIMOX substrate 202 including a buried layer of silicon dioxide 202b therein that define a (111) silicon surface layer 202c on an underlying (111) silicon substrate 202a. See Figure 16.
- the buried layer of silicon dioxide may be fabricated by implanting oxygen into a (111) silicon substrate to define a (11 1) silicon surface layer on the (11 1) silicon substrate. This process generally is referred to as SIMOX and is described for example in a publication entitled Silicon-on-
- a layer of 3C-silicon carbide 202d is epitaxially grown on the converted (111) silicon surface layer 202c' or directly on the (111) silicon surface layer 202c in a manner that was described above.
- the epitaxially grown layer of 3C-silicon carbide 202d optionally is thinned to produce a thinned epitaxial layer of 3C-silicon carbide 202d'.
- a 2H-aluminum nitride layer and/or gallium nitride buffer 202e then is grown on the thinned epitaxially grown layer of 3C-silicon carbide 202d'. Then, as shown in Figure 21 an underlying layer of 2H-gallium nitride
- Figures 22-26 now will show the use of pendeoepitaxy to laterally grow the underlying layer of 2H-gallium nitride 204 to thereby produce a gallium nitride microelectronic layer.
- epitaxial lateral overgrowth techniques of Figures 7-15, and/or other techniques may be used.
- the underlying gallium nitride layer 204 includes a plurality of sidewalls 205 therein.
- the sidewalls 205 may be thought of as being defined by a plurality of spaced apart posts 206, that also may be referred to as "mesas", “pedestals” or “columns”.
- the sidewalls 205 also may be thought of as being defined by a plurality of trenches 207, also referred to as "wells" in the underlying gallium nitride layer 204.
- the sidewalls 205 may also be thought of as being defined by a series of alternating trenches 207 and posts 206.
- a single post 206 may be provided, that may be thought of as being defined by at least one trench 207 adjacent the single post. It will be understood that the posts 206 and the trenches 207 that define the sidewalls
- the 205 may be fabricated by selective etching, selective epitaxial growth and/or other conventional techniques. Moreover, it also will be understood that the sidewalls need not be orthogonal to the substrate 202, but rather may be oblique thereto. Finally, it also will be understood that although the sidewalls 205 are shown in cross-section in Figure 22, the posts 206 and trenches 207 may define elongated regions that are straight, V-shaped or have other shapes. As shown in Figure 22, the trenches 207 may extend into the buffer layer 202e and into the silicon carbide layer 202c'/202d', so that subsequent gallium nitride growth occurs preferentially on the sidewalls 205 rather than on the trench floors.
- the trenches may not extend into the silicon carbide layer 202c7202d', and also may not extend into buffer layer 202e, depending, for example, on the trench geometry and the lateral versus vertical growth rates of the gallium nitride.
- the sidewalls 205 of the underlying gallium nitride layer 204 are laterally grown to form a lateral gallium nitride layer 208a in the trenches 207.
- Lateral growth of gallium nitride may be obtained at 1000-1100°C and 45 Torr.
- the precursors TEG at 13-39 ⁇ mol/min and NH 3 at 1500 seem may be used in combination with a 3000 seem H 2 diluent. If gallium nitride alloys are formed, additional conventional precursors of aluminum or indium, for example, may also be used.
- the term "lateral" means a direction that is orthogonal to the sidewalls 205. It will also be understood that some vertical growth on the posts 206 may also take place during the lateral growth from sidewalls 205.
- the term “vertical” denotes a directional parallel to the sidewalls 205.
- lateral gallium nitride layer 208a causes vertical growth onto the underlying gallium nitride layer 204, specifically onto the posts 206, to form a vertical gallium nitride layer 208b. Growth conditions for vertical growth may be maintained as was described in connection with Figure 23. As also shown in Figure 24, continued vertical growth into trenches 207 may take place at the bottom of the trenches.
- growth is allowed to continue until the lateral growth fronts coalesce in the trenches 207 at the interfaces 208c, to form a continuous gallium nitride semiconductor layer in the trenches.
- the total growth time may be approximately 60 minutes.
- microelectronic devices 210 may then be formed in the lateral gallium nitride semiconductor layer 208a. Devices also may be formed in vertical gallium nitride layer 208b. It will be understood that in the embodiments of Figures 16-26, a mask need not be used to fabricate the gallium nitride semiconductor structures because lateral growth is directed from the sidewalls 205. However, as will be described in connection with Figures 27-41, a mask may be used.
- an epitaxial lateral overgrowth then may be performed on the structure of Figure 26 using a mask as was described in connection with Figures 7-15. Laterally offset masks also may be used. Moreover, a second, laterally offset pendeoepitaxial process may be performed on the structure of Figure 26 by defining second trenches and/or posts. By performing two separate lateral growths, the defect density may be reduced considerably.
- a silicon substrate containing a buried oxide layer such as a SIMOX wafer 202 is used.
- the use of a SIMOX wafer can prevent or limit wa ⁇ ing of the substrate after formation of silicon carbide layers 202c'/202d'.
- the structures when the structures are cooled after silicon carbide formation from growth temperatures to room temperature, the structures may wa ⁇ due to the large mismatches in the coefficients of thermal expansion between silicon and silicon carbide. This effect may be more pronounced when using large diameter silicon wafers.
- using wafers with layers of oxide 202b may prevent or reduce the wa ⁇ ing by acting as a compliant substrate.
- the oxide may undergo viscous flow and accommodate the mismatches in both the lattice parameters and the coefficient of thermal expansion between the silicon and the silicon carbide layers. On cooling, the oxide layer may then provide a mechanism of strain relief and limit the wa ⁇ ing of the substrate.
- the silicon carbide 202c'/202d' is a preferred material template on which to grow the aluminum nitride buffer layer 202e and the gallium nitride semiconductor layers 204.
- Pendeoepitaxial growth of gallium nitride may be obtained on silicon carbide, because under the growth conditions used for pendeoepitaxial growth, gallium and nitrogen atoms generally will not bond to the silicon carbide surface in numbers and in time sufficient to cause gallium nitride nuclei to form.
- the silicon carbide layer may provide a diffusion barrier to prevent the interaction of silicon atoms with gallium and nitrogen species found in the growth environment. Referring now to Figures 27-41, third embodiments according to the present invention now will be described.
- SOI Semiconductor-On- Insulator
- microelectronic devices 301 including but not limited conventional CMOS devices, are fabricated in a (100) silicon substrate 302a using conventional techniques. It will be understood that the devices 301 may be formed later as well, as will be described in detail below. It also will be understood that microelectronic devices 301 may include optical and/or microelectromechanical (MEMS) devices as well.
- MEMS microelectromechanical
- the (100) silicon substrate 302a then is bonded to a (11 1) silicon substrate 302c using a bonding layer 302b and conventional bonding techniques.
- the bonding layer may be a microelectronic epoxy, a layer of silicon dioxide and/or other conventional materials.
- the (111) silicon substrate 302c is thinned to produce a (111) silicon layer 302c' on the (100) silicon substrate 302a.
- the operations of Figures 27-29 may form a conventional silicon on insulator (SOI) substrate 302 except that microelectronic devices 301 are contained therein.
- SOI silicon on insulator
- At least part of the (111) silicon layer 302c' is converted to 3C-silicon carbide layer 302c". As shown in Figure 30, all of the layer 302c' is converted to silicon carbide layer 302c". Moreover, as was described above, the conversion step may be eliminated. Then, as shown in Figure 31, a layer of 3C- silicon carbide 302d may be epitaxially grown on the converted (111) silicon layer 302c".
- the epitaxially grown layer of 3C-silicon carbide 302d is thinned to produce thinned layer 302d ⁇
- An aluminum nitride layer 302e then is grown on a thinned epitaxially grown layer of 3C-silicon carbide 302d'. This provides a platform 302' for subsequent growth of gallium nitride.
- a layer of 2H-gallium nitride 304 is grown on the aluminum nitride layer 302e.
- masked pendeoepitaxy is performed to laterally grow the layer of 2H-gallium nitride 304 to produce a gallium nitride microelectronic layer.
- maskless pendeoepitaxy, epitaxial lateral growth, other techniques and/or combinations thereof also may be used.
- a mask such as silicon nitride mask 309 is provided on the underlying gallium nitride layer 304.
- the mask 309 may have a thickness of about 1000 Angstroms and may be formed on the underlying gallium nitride layer 304 using low pressure chemical vapor deposition (CVD) at 410°C.
- CVD low pressure chemical vapor deposition
- the underlying gallium nitride layer 304 includes a plurality of sidewalls 105 therein.
- the sidewalls 305 may be thought of as being defined by a plurality of spaced apart posts 306, that also may be referred to as "mesas",
- the sidewalls 305 may also be thought of as being defined by a plurality of trenches 307, also referred to as "wells" in the underlying gallium nitride layer 304.
- the sidewalls 305 may also be thought of as being defined by a series of alternating trenches 307 and posts 306. It will be understood that the posts 306 and the trenches 307 that define the sidewalls 305 may be fabricated by selective etching, selective epitaxial growth and/or other conventional techniques. Moreover, it also will be understood that the sidewalls need not be orthogonal to the substrate 302, but rather may be oblique thereto.
- the posts 306 and trenches 307 may define elongated regions that are straight, V-shaped or have other shapes.
- the trenches 307 preferably extend into the buffer layer 302e and into the silicon carbide layer 302d'/302c", so that subsequent gallium nitride growth occurs preferentially on the sidewalls 305 rather than on the trench floors.
- the trenches may not extend into the silicon carbide layer 302d'/302c", and also may not extend into the buffer layer 302e.
- the sidewalls 305 of the underlying gallium nitride layer 304 are laterally grown to form a lateral gallium nitride layer 308a in the trenches 307.
- Lateral growth of gallium nitride may be obtained at about 1000- 1100°C and about 45 Torr.
- the precursors TEG at about 13-39 ⁇ mol/min and NH 3 at about 1500 seem may be used in combination with about 3000 seem H 2 diluent. If gallium nitride alloys are formed, additional conventional precursors of aluminum or indium, for example, also may be used.
- the term "lateral" means a direction that is parallel to the faces of the substrate 302'.
- lateral gallium nitride 308a may also take place during the lateral growth from the sidewalls 305.
- vertical denotes a directional parallel to the sidewalls 305.
- Conditions for vertical growth may be maintained as was described above. As also shown in Figure 37, continued vertical growth into trenches 307 may take place at the bottom of the trenches.
- lateral gallium nitride layer 308a causes lateral overgrowth onto the mask 309, to form lateral overgrowth gallium nitride layer 308b. Growth conditions for overgrowth may be maintained as was described above.
- growth is allowed to continue until the lateral overgrowth fronts coalesce over the mask 309 at the interfaces 308d, to form a continuous gallium nitride semiconductor layer.
- the total growth time may be approximately 60 minutes.
- microelectronic devices 310 may then be formed in the lateral gallium nitride semiconductor layer 308a. Devices may also be formed in lateral overgrown gallium nitride layer 308b.
- the microelectronic devices 301 in the (100) silicon substrate then may be electrically connected to the microelectronic devices 310 in the pendeoepitaxial gallium nitride layer to provide an integrated optical and electronic substrate.
- the connection may use conventional metalization soldering and/or other techniques. Accordingly, high density integrated optoelectronic devices may be formed using conventional (100) silicon SOI substrates.
- the silicon carbide layer 302d'/302c" may be critical to the success of forming gallium nitride structures because the silicon carbide is a preferred material template on which to grow the aluminum nitride layer 302e and the gallium nitride semiconductor layer 304. Moreover, under the growth conditions used for pendeoepitaxial growth, gallium and nitrogen atoms generally will not bond to the silicon carbide surface in numbers and times sufficient to cause gallium nitride nuclei to form. Alternatively, it will be understood that the bottom of the trenches 307 may be masked, for example with silicon nitride. The silicon carbide layer also may provide a diffusion barrier to prevent the interaction of silicon atoms with gallium and nitrogen species found in the growth environment.
- the SOI wafers can prevent or limit wa ⁇ ing of the substrate after silicon carbide formation.
- the bonding layer 302b may prevent or limit the wa ⁇ ing by acting as a compliant substrate.
- the bonding layer 302b may also provide a mechanism of strain relief and may limit the wa ⁇ ing of the substrate.
- FIGS 42-45 other embodiments of gallium nitride semiconductor structures and fabrication methods according to the present invention will now be described.
- the structures use different spacings or dimensions for the posts and trenches.
- a small post- width/trench width ratio is used.
- discreet gallium nitride structures shown in Figure 42 may be obtained.
- a large post-width/trench-width ratio is used so that gallium nitride structures shown in Figure 44 may be obtained.
- gallium nitride semiconductor structures of Figure 42 are fabricated as was already described.
- growth is allowed to continue until the lateral overgrowth fronts coalesce over the mask 309 at the interface 308b to form a continuous gallium nitride semiconductor layer over the mask 309.
- the total growth time may be approximately 60 minutes.
- microelectronic devices 310 may be formed in the lateral overgrowth gallium nitride layer 308d.
- at least some of the discreet gallium nitride structures are removed to expose the microelectronic devices 301 in the (100) silicon substrate 302a.
- Figure 44 using a large post- width/trench-width ratio, gallium nitride semiconductors structures of Figure 44 are fabricated as was already described.
- growth is allowed to continue until the lateral overgrowth fronts coalesce in the trench 307 at the interfaces 308c to form a continuous gallium nitride semiconductor layer 308a over the trench 307.
- the total growth time may be approximately 60 minutes.
- microelectronic devices 310 may be formed in the pendeoepitaxial gallium nitride layer 308a.
- at least a portion of the gallium nitride structure may be removed to thereby expose the underlying microelectronic devices 301, and was described above.
- devices 301 are formed in the (100) silicon substrate 302a prior to forming the gallium nitride devices 310.
- gallium nitride fabrication processes may occur at temperatures that are sufficiently high to destroy or degrade performance of the silicon devices 301 due to diffusion or other thermal effects. Accordingly, it may be desirable to form the microelectronic devices 301 in the (100) silicon substrate 302a after forming the gallium nitride layers and structures.
- Figures 46-49 illustrate methods of forming microelectronic devices in the (100) silicon substrate after forming the gallium nitride layers and structures.
- the structure of Figure 45 may be fabricated except that microelectronic devices 301 are not formed until after the gallium nitride structures are formed.
- the face of the (100) silicon substrate 302a is exposed, and conventional microelectronic devices 301 may be formed in the exposed surface. It may be difficult to fabricate the microelectronic devices 301 within the trenches between the gallium nitride devices.
- the embodiments of Figures 47-49 illustrate alternative fabrication techniques that need not fabricate the silicon microelectronic devices 301 at the bottom of the trenches.
- the device of Figure 45 is fabricated except that microelectronic devices 301 are not fabricated in the (100) silicon substrate 302a.
- a capping layer 320 for example silicon dioxide and/or silicon nitride, then is formed on the gallium nitride devices.
- the (100) silicon substrate 302a is selectively epitaxially grown to form a (100) silicon layer 302a*.
- Devices 301' then are formed in the epitaxially grown silicon layer 302a'.
- the devices 301' may be formed at the surface of the structure rather than at the floor of a trench.
- the capping layer 320 optionally may be removed to provide a free-standing silicon layer 302a' that is separated from the gallium nitride-based structures.
- the devices may be connected using metallization at the top surface.
- metallization within or on the (100) silicon substrate 302a may be provided.
Abstract
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AU21520/00A AU2152000A (en) | 1998-11-24 | 1999-11-18 | Fabrication of gallium nitride layers on silicon |
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US6764932B2 (en) | 1999-10-14 | 2004-07-20 | Cree, Inc. | Single step pendeo- and lateral epitaxial overgrowth of group III-nitride epitaxial layers with group III-nitride buffer layer and resulting structures |
US6803602B2 (en) | 1999-10-14 | 2004-10-12 | Cree, Inc. | Single step pendeo- and lateral epitaxial overgrowth of Group III-nitride epitaxial layers with Group III-nitride buffer layer and resulting structures |
US6812053B1 (en) | 1999-10-14 | 2004-11-02 | Cree, Inc. | Single step pendeo- and lateral epitaxial overgrowth of Group III-nitride epitaxial layers with Group III-nitride buffer layer and resulting structures |
US6955977B2 (en) | 1999-10-14 | 2005-10-18 | Cree, Inc. | Single step pendeo-and lateral epitaxial overgrowth of group III-nitride epitaxial layers with group III-nitride buffer layer and resulting structures |
US7361576B2 (en) | 2005-05-31 | 2008-04-22 | The Regents Of The University Of California | Defect reduction of non-polar and semi-polar III-Nitrides with sidewall lateral epitaxial overgrowth (SLEO) |
US7955983B2 (en) | 2005-05-31 | 2011-06-07 | The Regents Of The University Of California | Defect reduction of non-polar and semi-polar III-nitrides with sidewall lateral epitaxial overgrowth (SLEO) |
US9257342B2 (en) | 2012-04-20 | 2016-02-09 | Infineon Technologies Ag | Methods of singulating substrates to form semiconductor devices using dummy material |
US9741618B2 (en) | 2012-04-20 | 2017-08-22 | Infineon Technologies Ag | Methods of forming semiconductor devices |
CN105247665A (zh) * | 2013-05-31 | 2016-01-13 | 三垦电气株式会社 | 半导体装置 |
US9406564B2 (en) | 2013-11-21 | 2016-08-02 | Infineon Technologies Ag | Singulation through a masking structure surrounding expitaxial regions |
Also Published As
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US6255198B1 (en) | 2001-07-03 |
US6602764B2 (en) | 2003-08-05 |
AU2152000A (en) | 2000-06-13 |
US20020031851A1 (en) | 2002-03-14 |
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